[0001] The present invention relates to sanitizer compositions, and in particular to such
compositions containing a peroxyacid species, and additionally to processes for sanitization
employing such compositions:
The sanitizer compositions described herein are primarily directed towards the sanitization
and cleansing of reusable nappies, sometimes referred to as babies napkins and in
America as diapers, but such compositions can also be used for other apparel, soiled
linen or fabrics or for surfaces which may have come into contact with human or animal
excrements. The problems of sanitization of nappies is of especial importance in view
of the subsequent intimate and prolonged contact between a reused nappy and the baby
and the vulnerability particularly of young babies to infection. Consequently, there
is constantly a need to provide new and effective nappy sanitizer compositions. Furthermore,
the natural pride of parents in their offspring lead them to seek sanitizing compositions
offering a cleansed and bright appearance for the nappies in addition to sanitization.
[0002] French Patent Specification No. 1 568 918 to Vick International Limited describes
washing and disinfecting compositions for babies nappies which comprise potassium
monopersulphate, sodium chloride, a surfactant and detergent builders. Such compositions
were available commercially from Richardson Vick in 1982 but when tested performed
poorly in a recent test for nappy sanitizing compositions, Australian Standard 2351.
[0003] European Patent Specification 27693 to Interox Chemicals Limited describes the preparation
of various magnesium salts of percarboxylic acid/carboxylate compounds including magnesium
monoperoxyphthalate and washing compositions containing them but makes no reference
to the inclusion of an alkali metal chloride in such compositions and indeed on page
6 excludes salts of halogen acids from the class of diluents to employ with the invention
magnesium salts.
[0004] According to the present invention there is provided a sanitizer composition comprising
a peroxygen compound, an alkali metal chloride, surfactant and detergent builder characterised
in that it contains from 5 to 20% of magnesium monoperoxyphthalate, 30 to 60% alkali
metal chloride, 3 to 15% anionic surfactant, 0 to 20% nonionic ethoxylated surfactant,
10 to 50% detergent builder or builders and 0 to 5% of a complexing builder.
[0005] Herein, % is by weight, based on the composition unless stated otherwise.
[0006] The components of such compositions are usually included in particulate form, the
particle ranges in practice being selected so as to avoid if possible substantial
segregation of the components during transport or storage.
[0007] It will be observed that invention compositions contain both the peroxyacid compound
and an alkali metal chloride, which can interact in aqueous solution to generate oxychlorine
species, of which the nature of the predominating species will vary depending upon
the pH of the solution.
[0008] The alkali metal chloride is preferably sodium chloride in view of its widespread
availability in crystalline form. In many invention compositions, the ratio of alkali
metal chloride to peroxygen compound is from 1:1 to 20:1.
[0009] By magnesium monoperoxyphthalate, we mean herein the compound having the empirical
formula

[0010] It will be recognised that the salt is that of the carboxylate group only, that the
peroxy group remains in acid form. The aforementioned magnesium salt, which for the
sake of brevity may be referred to herein alternatively as MMPP, demonstrates good
storage stability itself.
[0011] The magnesium monoperoxyphthalate can be prepared by the method described in European
Patent Specification 27693, the resultant crystalline material being hydrated, x-ray
diffraction data indicating a hexahydro magnesium structure.
[0012] In practice, the method of manufacture of MMPP often results in the particles of
the peroxygen compound containing a small proportion of the corresponding non-peroxygenerated
compound. Thus for MMPP, a small proportion of magnesium phthalate can be present.
[0013] In order to enhance the cleansing performance of the composition it includes one
or more surfactants. The surfactants can be soaps or be synthetic, for example as
described in chapter 2 of Synthetic Detergents by A Davidsohn and B M Milwidsky, 5th
Edition published in 1972 by Leonard Hill, London, and methods of making them are
described in chapter 4 of the same book.
[0014] Amongst anionic surfactants described on pages 15-23 of the aforementioned book,
sulphonates and sulphates are of special practical importance. The sulphonates includes,
for example, alkaryl sulphonates, and particularly alkyl benzene sulphonates, the
alkyl group preferably being straight chain containing 9 to 15 carbon atoms, of which
one of the most commonly employed surfactants is linear dodecyl benzene sulphonate.
Other anionic sulphonates which are useful in washing compositions containing MMPP
include olefin sulphonates, obtained, for example, by sulphonating primary or secondary
aliphatic monoolefins, alkene sulphonates, especially linear alkene sulphonates, and
hydroxy alkene sulphonates and disulphonates, especially 3-, 4-, and 5-, hydroxy-n-alkyl
sulphonates in which the alkyl group contains any even number from 10 to 24 carbon
atoms. Other desirable anionic surfactants include alcohol sulphates, preferably linear,
having a chain length of at least 10 carbon atoms and sulphated fatty acid alkanolamides.
Other sulphates comprise sulphated nonionic surfactants as for example alkylphenyl-ethylene
oxide ether sulphate in which the alkyl groups contain from about 8 to 12 carbon atoms
and there are 1 to 10 units of ethylene oxide in each molecule. Yet other sulphate
surfactants comprise alkyl ether sulphates where the alkyl group contains from 10
to 20 carbon atoms, preferably linearly and each molecule contains from 1 to 10 preferably
from 1 to 4 molecules or ethylene oxide. Further anionic surfactants include phosphate
derivatives of the ethylene oxide based nonionic surfactants described herein.
[0015] Many of the suitable nonionic surfactants comprise condensation products of ethylene
oxide and possibly propylene oxide. One class of such nonionic surfactants which is
of special importance comprises water soluble condensation products of alcohols containing
from 8 to 18 carbon atoms with an ethylene oxide polymer often containing at least
10 molecules of ethylene oxide per molecule of surfactant, e.g. from 10 to 30 moles
of ethylene oxide. Particularly desirable nonionic surfactants comprise water soluble
condensates of alkyl phenols or alkyl naphthols with an ethylene oxide polymer normally
containing from 5 to 25 moles of ethylene oxide per mole of alkyl phenol or alkyl
naphthol. The alkyl group normally contains from 6 to 12 carbon atoms and is frequently
linear.
[0016] As an alternative to the hydrophobic moiety of the nonionic surfactant being linked
to the hydrophilic moiety by an ether link as in alkyl phenol ethylene oxide condensates,
the linkage can be an ester group. The hydrophobic moiety is normally the residue
of a straight chain aliphatic acid containing from 10 to 22 carbon atoms and more
particularly lauric, stearic and oleic residues. In one class of nonionic ester surfactants,
the hydrophilic moiety comprises polyethylene oxide, frequently in the ratio of from
5 to 30 moles of ethylene oxide per mole of the fatty acid residue. It will be recognised
that both mono and di esters can be employed. Alternatively it is possible to employ
as the hydrophilic moiety glycerol, thereby producing either mono- or di-glycerides.
In a further group, the hydrophilic moiety comprises sorbitol. A further class of
nonionic surfactants comprise alkanolamides in which a C10 to C22 amide is condensed
with a polyethylene oxide or polypropylene glycol hydrophilic moiety or moieties.
Semi-polar detergents include water soluble amine oxides, water soluble phosphine
oxides and water soluble sulphur oxides, each containing one alkyl moiety of from
10 to 22 carbon atoms and two short chain moieties selected from the groups of alkyl
and hydroxyalkyl groups containing 1 to 3 carbon atoms.
[0017] The nonionic and anionic surfactants are often employed together, in many cases in
a weight ratio within the range 2:1 to 1:10.
[0018] The surfactants provide in total in many embodiments from 1 to 25% of the composition.
[0019] A further component of the compositions of the present invention is a builder or
mixture of builders, elsewhere alternatively referred to as detergent builders. It
will be understood that such compounds can perform several different roles during
use of the composition, including one or more of detergent enhancement, peptisation,
water softening, sequestration of catalytic metals, pH adjustment, and percompound
stabilisation. The skilled chemist in cleansing, bleaching and sanitizing compositions
will naturally recognise which of the foregoing roles are provided by each of the
subsequently listed builders, and he will of course select the builder and the form
of the builder, i.e. either acid or alkaline salt form in accordance with standard
knowledge to obtain his desired pH in the sanitizing solution and his desired combination
of properties. Many of the suitable builders are water soluble. These include alkali
metal phosphates, often being pyrophosphates, tripolyphosphates, or higher polymetaphosphates,
the latter of which include hexametaphosphates and alkali metal hydrogen phosphates.
They also include alkali metal carbonates and bicarbonates and borates. Water insoluble
inorganic builders include zeolites, especially zeolites A and X. As is conventional,
the alkali metal is preferably sodium in such builders.
[0020] The builder can also be organic and such builders include hydroxycarboxylic acids,
polycarboxylic acids, aminocarboxylic acids and phosphonic acids or their alkali metal,
especially sodium salts thereof. Such organic builders are often loosely referred
to as complexing builders. It will be recognised that the classes overlap to some
extent. Suitable examples of such complexing builders, listed in acid form for brevity,
include C
2 to C
'o alpha-omega dicarboxylic acids, 1,1,3,3-propane tetracarboxylic acid, oxydiacetic
acid, citric acid, tartaric acid, gluconic acid, oxydisuccinic acid, furan tetracarboxylic
acid and polymeric carboxylic acid compounds obtained from e.g. acrylic acid, hydroxyacrylic
acid or maleic acid. Other examples include nitrilotriacetic acid (NTA), ethylenediaminetetraacetic
acid (EDTA), diethylenetriaminepentaacetic acid (DTPA) and their counterparts in which
the acetic acid group is replaced by a 2-hydroxyethyl group, or a methylene (phosphonic
acid) group (NTMP, EDTMP, DTPMP). Further examples include 1-hydroxyethane-1,1-diphosphonic
acid (HEPA). These exemplified builders are representative of the various sub-classes
of builders, and often they are used as the sodium salt.
[0021] The total amount of builder is in the range of 10 to 50%, of which at least a part
is a phosphate in many embodiments in view of its combination of useful properties,
and often from 5 to 25% of the composition. The complexing builders, when used, tend
to be selected within the range of 0.1% to 5% of the composition, and often are included
as a complement to the inorganic builder or builders.
[0022] In some preferred embodiments, the composition comprises:
(a) from 5 to 20% of MMPP;
(b) from 30 to 60% sodium chloride;
(c1) from 3 to 15% anionic surfactant, such as a linear C9-C15 alkyl benzene sulphonate, sodium salt;
(c2) from 0 to 20% of a nonionic ethoxylated surfactant; and
(d1) from 5 to 30% of a phosphate builder, sodium salt;
(d2) from 5 to 30% of a non-phosphate inorganic builder, such as sodium carbonate
or bicarbonate or borax; and
(d3) from 0 to 5% of an organic complexing builder such as NTA, EDTA, EDTMP, DTPMP
or gluconate or mixture of two or more thereof.
[0023] In addition to the foregoing components, the composition can include also one or
more auxiliary agents, such as alkaline sulphates - e.g. sodium sulphates from 0 to
40% of the composition and in minor amounts soil anti-redeposition agents such as
CMC or PVP, dyes, perfumes, dye transfer inhibitors and optical brightening agents.
These minor auxiliary components often comprise from 0 to 20% in total, in many cases
from 1 to 10%. In this context it will be understood that small concentrations of
phosphonates, gluconate and aminocarboxylates alone or in combination in a total amount
of for example as low a range as 0.2 to 2.0% can stabilise the peroxygen compound
in solution. Other peroxygen stabilisers like dipicolinic acid or hydroxy quinoline
can also be used.
[0024] The compositions are under normal storage conditions in the form of mixtures of solid
particles. Accordingly they can be made in conventional equipment for blending and
mixing powders. It will also be recognised that the components other than the peroxygen
compound can be pre-blended together, to any desired extent, in slurry which is subsequently
dried, e.g. spray dried and thereafter blended with the peroxygen compound. Accordingly
also, the surfactant can often be introduced into the pre-mixture in liquid form.
[0025] The compositions are employed in a dilute aqueous solution, often at a concentration
of 1 to 20 g/I, in which many of them generate a pH preferably within the range of
pH 7.8 to 11. The solution is often made at up to hand hot temperatures, such as from
25 to 45°C, although higher temperatures could be used and thereafter allowed to cool
to ambient or maintained within that range. The solution can be replaced periodically,
such as daily and if desired the concentration of sanitizer composition can be augmented
from time to time, e.g. to restore the available oxygen level to around its original
level. For more general washing uses any temperature from ambient to boiling point
can be employed, preferably using a solution having an initial avox of at least 5
ppm. For cleaning many surfaces a slurry or paste can be used instead of a solution,
if desired.
[0026] Prolonged contact between the aqueous mixtures of the invention compositions and
steel surfaces is not recommended.
[0027] Having described the invention in general terms, an embodiment thereof will now be
given in greater detail by way of example only.
Examples
[0028] In the Examples, sanitizer compositions were produced by blending together in a mixer,
dry powders for a, b, d1 and d2 and an aqueous solution of c to give on a dry weight
basis the following compositions:
(a) magnesium monoperoxyphthalate (avox of 5.9% w/w of the MMPP granules)
(b) sodium chloride
(c) linear dodecyl benzene sulphonate (NANSA SS30)
(d1) sodium tripolyphosphate
(d2) sodium carbonate
(d3) sodium bicarbonate

[0029] In Examples 1 to 3, the solution obtained had a pH of over 10, and in Examples 4
to 6 of about pH 8.1.
[0030] The sanitizing capability of each composition was tested by dissolving it at 37°C
initial temperature in water at 4.4 g/l, and determining the survival of standard
bacteria, Escherichia Coli (NCTC 8196) and Staphylcoccus Aureus (NCTC 4163) under
the stimulated use conditions of the Standards Association of Australia, Australian
Standard 2351 - 1980 Nappy Sanitizers. The results of faecal challenges at the Start
(to) and End (t
5), measured at time 7 hours are given below. Certain minor modifications were made
to the standard procedure, namely the use of innoculated agar slopes instead of a
centrifuged broth to provide the bacterial suspension, and the use of the pour plate
technique using 1 ml aliquots introduced, incubated at 37°C for 48 hours, instead
of the spread dry technique, 0.5 ml aliquots and incubation at 30°C for 72 hours.
[0031] In the tests, a 700 ml sample of sanitizing solution was used with 6 nappies.
[0032] By way of comparison in comparison A, a commercial nappy sanitizer composition of
similar composition, but containing an inorganic peracid salt instead of MMPP, was
tested using the same modified procedure and conditions. The commercial product was
analysed to approximately:

[0033] The persulphate triple salt has the formula 2KH.SO
5.K
2SO
4.KHS0
4 and has a nominal 6% avox.

[0034] The initial bacterial concentrations were always about 2.5 to 3.4x 1 07 CFU/cm
3, and -10 indicates that the concentration was below 10.
[0035] From Table 2, it can be seen that the invention product performed substantially better
than the commercial peracid-containing comparison product A. Similar results were
obtained on repetition of the trials.
[0036] Examples 2 to 6 were compared using the same test procedure with a further commercially
available sanitizing composition (B) which on analysis was very similar to the formulation
on page 9 of European Patent Specification 47015 (Richardson-Vicks Pty) containing
over 25% w/w sodium percarbonate, i.e. an avox content of approximatley 6 times that
of Example 1.
[0037] The results are summarised in Table 3

[0038] From Table 2, it can be seen that the invention products within the limits imposed
by microbiological test procedures were demonstrably better than comparison B even
though the latter contained often about 10 times as much avox (active oxygen). It
was also noticed that for many of the Example compositions, if a slightly longer soak
(an extra 1 or 2 hours) was used, a further substantial fall in bacterial count to
below or near 100 CFU cm-
3 occurred.